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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Slc35d1tm1Hko
targeted mutation 1, Haruhiko Koseki
MGI:3774133
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Slc35d1tm1Hko/Slc35d1tm1Hko involves: 129S1/Sv * 129X1/SvJ MGI:3812126


Genotype
MGI:3812126
hm1
Allelic
Composition
Slc35d1tm1Hko/Slc35d1tm1Hko
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc35d1tm1Hko mutation (0 available); any Slc35d1 mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

skeleton
• at birth, mice exhibit hypoplasia of the craniofacial bones (J:130304)
• at birth, mice exhibit hypoplasia of the craniofacial bones (J:130304)
• at E15.5, the proliferating zone is greatly reduced compared to in wild-type mice and the cartilage within it is disorganized (J:130304)
• however, proliferation and apoptosis rates as well as chondrocyte differentiation within the zone are normal (J:130304)
• at E15.5, the proliferating zone is greatly reduced compared to in wild-type mice and the cartilage within it is disorganized (J:130304)
• however, proliferation and apoptosis rates as well as chondrocyte differentiation within the zone are normal (J:130304)
• longitudinally short (J:130304)
• longitudinally short (J:130304)
• flattened (J:130304)
• flattened (J:130304)

growth/size/body
• narrow (J:130304)
• narrow (J:130304)

limbs/digits/tail
• extremely short limbs (J:130304)
• extremely short limbs (J:130304)

craniofacial
• at birth, mice exhibit hypoplasia of the craniofacial bones (J:130304)
• at birth, mice exhibit hypoplasia of the craniofacial bones (J:130304)

digestive/alimentary system

Mouse Models of Human Disease
OMIM ID Ref(s)
Schneckenbecken Dysplasia 269250 J:130304





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last database update
02/02/2016
MGI 6.02
The Jackson Laboratory